‘NAME. DATE. Chap 20 Acid and Base Worksheet 1. In each ofthe following, i 5 identity the acd bse, conugne ai, and conjugate bate: NH, + OH + NH) + HO 2, What is the {1H ] in @ 0.25 M solution of NaOH (strong). ‘What is [0H] P | Since Nach tees trom, ba ae CoH’, ey | mS at poe” | Noo A Mat ror” oh) cytqs O'Aos t 3. Caleulate the [H") end [O41] ina 0.50 M solution of HNO, (oro. Staw BNOs is st¥one CH NOS) ye Cou e265 =l2e xl A 4. Calculate the [H ] end [OH] ina 0.35 M HCIO, solution (strong). ret] 235M, Coots 2e6xX1O A 5. KOH is strong base. Calculate [1] and [O11] in a 5.0 M solution, cowl = SoM ' cat} exci 6 Case the pH and pOH of Solution of NaOH (strong base) Which i 0.0010 M. gow o00iM pote 3 pHs (4-320 at cH] =< jx io M 7-Caleiatehe(]ofsouion witha p51 ~37 i Cutle (p77) = zeoxot uy 8. Calculate the [IT ] ofa solution with a pOHT of 4.5 pe 14-he oa cat yy to = 316 x10 My9. Calculate iH] in 2.0.10 M solution of formic acid, ope ea ae Cu 7 Hc OOH, ctcHocvo” + 47. oH) os q> t 0,100M ° 2 ¢ ~* x a E pi- ww Ol i : Kae tay io ie smett i Beery i fy ur 3 Baws = Sy gy 1b&s > (ew = Dex ut 12. Many of the common organic acids got their original names from their odors and/or sources. Another casein pont is Capric acid (hexanoie acid), found inthe skin Seeetions 0 goats (L. caper, goal). Caproic acid is CH (CH) COOH and ‘has a structure similar to acetic acid, but with a longer carbon chain. The concentration of Hin a solution prepared by dissolving 0.030 mol of caproic acid in 1.01. of water solution was measured and found tobe 6.5 x 10" M. Find K, for eproi ai i CH3 (CHa Cood —> CH3fctalycos tH 3p Cota oO oO x x aa GS x6 63X10